F. Tihy

F. Glorieux, M. Labuda, F. Tihy, 1993, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

NUP98‐BPTF gene fusion identified in primary refractory acute megakaryoblastic leukemia of infancy

P. Gendron, B. Wilhelm, E. Lemyre, 2018, Genes, chromosomes & cancer.

Whole‐genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype

E. Lemyre, V. Désilets, J. Michaud, 2012, Clinical genetics.

CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems

S. Scherer, A. C. Lionel, C. Marshall, 2014, Journal of Neurodevelopmental Disorders.

Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay

S. Scherer, D. Merico, C. Marshall, 2016, Scientific Reports.

De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype.

E. Lemyre, F. Tihy, N. Lemieux, 1999, American journal of medical genetics.

PTPRD copy number variants and Ewing's sarcoma: Strengthening the association and therapeutic implications.

E. Lemyre, L. Armstrong, F. Tihy, 2019, Cancer genetics.

Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability

I. Deary, T. Bourgeron, C. Greenwood, 2021, Molecular Psychiatry.

Genome wide analysis of gene dosage in 24,092 individuals shows that 10,000 genes modulate cognitive ability

I. Deary, T. Bourgeron, C. Greenwood, 2020, bioRxiv.

Genome wide analysis of gene dosage in 24,092 individuals shows that 10,000 genes modulate cognitive ability

I. Deary, T. Bourgeron, C. Greenwood, 2020, bioRxiv.

Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada

D. Stavropoulos, Jo-Ann K. Brock, W. Gibson, 2018, Journal of Medical Genetics.

SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay

E. Lemyre, M. Srour, G. Mathonnet, 2014, BMC Medical Genomics.

Cytogenetic analysis of a parachordoma.

P. Russo, F. Tihy, N. Lemieux, 1998, Cancer genetics and cytogenetics.

Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p.

E. Lemyre, F. Tihy, N. Lemieux, 2000, American journal of medical genetics.

Frequencies of chromosomal abnormalities at amniocentesis: over 20 years of cytogenetic analyses in one laboratory.

F. Tihy, L. Dallaire, L. Caron, 1999, American journal of medical genetics.

Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35.

M. Econs, C. Kos, F. Tihy, 1994, Genomics.

Comparative RB1 gene mapping in Homo sapiens, Pithecia pithecia, Macaca sylvana, and Cercopithecus aethiops tantalus.

B. Dutrillaux, M. Lombard, F. Tihy, 1996, Cytogenetics and cell genetics.

Activation of the catalytic core of a group I intron by a remote 3' splice junction.

E. Westhof, L. Jaeger, F. Michel, 1992, Genes & development.

The microcell-mediated transfer of human chromosome 8 restores the deficient N-acetylytransferase activity in skin fibroblasts of Mucopolysaccharidosis type IIIC patients

A. Pshezhetsky, F. Tihy, V. Seyrantepe, 2006, Human Genetics.

Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughter

B. Dutrillaux, F. Leturcq, J. Kaplan, 1994, Human Genetics.

Complex chromosome rearrangement and recombinant balanced translocation in a mother and a daughter with the same phenotypic abnormalities

E. Lemyre, F. Tihy, N. Lemieux, 2005, American journal of medical genetics. Part A.

Carrier screening for genetic disorders in individuals of Ashkenazi Jewish descent.

S. Langlois, V. Désilets, A. Summers, 2006, Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC.